An Open-Label, Multicenter Study to Evaluate the Pharmacokinetics, Safety, and Efficacy of Glecaprevir/Pibrentasvir in Pediatric Subjects with Genotypes 1-6 Chronic Hepatitis C Virus (HCV) Infection
		
	
		
			
				| Sponsor: | AbbVie, Inc. | 
			
			
				| Enrolling: | Male and Female Patients | 
							
					| Study Length: | 160 Weeks | 
						
							
					| Clinic Visits: | 13 | 
			
			
                            
                    | IRB Number: | AAAR2252 | 
            
			 
				
					| U.S. Govt. ID: | NCT03067129 | 
					
			
				| Contact: | Danilo Gamino: 212-305-6758 / dg3031@cumc.columbia.edu | 
		
	
		Open-labeled hepatitis C pediatric treatment trial with a two drug direct acting viral oral combination (already approved in adults) across all genotypes for naive or treatment experienced subjects.
	
			This study is closed
	
	   	
		Investigator
		
		Steven Lobritto, MD
		
					   
	
		
		
		
			
				
					| Has your child been diagnosed with Hepatitis C virus? | Yes | No | 
				
									
						| Has your child tested positive for Hepatitis B? | Yes | No |